-
1
-
-
0000269268
-
Associated non cardiac malformations in children with congenital heart disease
-
Noonan JA, Ehmke DA: Associated non cardiac malformations in children with congenital heart disease. J Pediatr 1963;63:468-470.
-
(1963)
J Pediatr
, vol.63
, pp. 468-470
-
-
Noonan, J.A.1
Ehmke, D.A.2
-
2
-
-
0028127042
-
Clinical and molecular studies in a large Dutch family with Noonan syndrome
-
van der Burgt I, Berends E, Lommen E, van Beersum S, Hamel B, Mariman E: Clinical and molecular studies in a large Dutch family with Noonan syndrome. Am J Med Genet 1994;53:187-191.
-
(1994)
Am J Med Genet
, vol.53
, pp. 187-191
-
-
van der Burgt, I.1
Berends, E.2
Lommen, E.3
van Beersum, S.4
Hamel, B.5
Mariman, E.6
-
3
-
-
33751257771
-
The cardiofaciocutaneous syndrome
-
Roberts A, Allanson J, Jadico SK, Kavamura MI, Noonan J, Opitz JM, Young T, Neri G: The cardiofaciocutaneous syndrome. J Med Genet 2006;43:833-842.
-
(2006)
J Med Genet
, vol.43
, pp. 833-842
-
-
Roberts, A.1
Allanson, J.2
Jadico, S.K.3
Kavamura, M.I.4
Noonan, J.5
Opitz, J.M.6
Young, T.7
Neri, G.8
-
4
-
-
27144531386
-
Germline mutations in HRAS pro to-oncogene cause Costello syndrome
-
Aoki Y, Niihori T, Kawame H, Kurosawa K, Ohashi H, Tanaka Y, Filocamo M, Kato K, Suzuki Y, Kure S, Matsubara Y: Germline mutations in HRAS pro to-oncogene cause Costello syndrome. Nat Genet 2005; 37: 1038-1040.
-
(2005)
Nat Genet
, vol.37
, pp. 1038-1040
-
-
Aoki, Y.1
Niihori, T.2
Kawame, H.3
Kurosawa, K.4
Ohashi, H.5
Tanaka, Y.6
Filocamo, M.7
Kato, K.8
Suzuki, Y.9
Kure, S.10
Matsubara, Y.11
-
5
-
-
0014337419
-
Direct familial transmission of the Turner phenotype
-
Nora JJ, Sinha AK: Direct familial transmission of the Turner phenotype. Am J Dis Child 1968;116:343-350.
-
(1968)
Am J Dis Child
, vol.116
, pp. 343-350
-
-
Nora, J.J.1
Sinha, A.K.2
-
6
-
-
0028077697
-
Mapping a gene for Noonan syndrome to the longarm of chromosome 12
-
Jamieson CR, van der Burgt I, Brady AF, van Reen M, Elsawi MM, Hoi F, Jeffery S, Patton MA, Mariman E: Mapping a gene for Noonan syndrome to the longarm of chromosome 12. Nat Genet 1994;8:357-360.
-
(1994)
Nat Genet
, vol.8
, pp. 357-360
-
-
Jamieson, C.R.1
van der Burgt, I.2
Brady, A.F.3
van Reen, M.4
Elsawi, M.M.5
Hoi, F.6
Jeffery, S.7
Patton, M.A.8
Mariman, E.9
-
7
-
-
18344385476
-
Mutations in PTPN11, encodingthe protein tyrosine phosphatase SHP-2, cause Noonan syndrome
-
Tartaglia M, Mehler EL, Goldberg R, Zampino G, Brunner HG, Kremer H, van der Burgt I, Crosby AH, Ion A, Jeffery S, Kalidas K, Patton MA, Kucherlapati RS, Gelb BD: Mutations in PTPN11, encodingthe protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat Genet 2001;29:465-468.
-
(2001)
Nat Genet
, vol.29
, pp. 465-468
-
-
Tartaglia, M.1
Mehler, E.L.2
Goldberg, R.3
Zampino, G.4
Brunner, H.G.5
Kremer, H.6
van der Burgt, I.7
Crosby, A.H.8
Ion, A.9
Jeffery, S.10
Kalidas, K.11
Patton, M.A.12
Kucherlapati, R.S.13
Gelb, B.D.14
-
8
-
-
33644622238
-
Germline KRAS mutations cause Noonan syndrome
-
Schubbert S, Zenker M, Rowe SL, Boll S, Klein C, Bollag G, van der Burgt I, Musante L, Kalscheuer V, Wehner LE, Nguyen H, West B, Zhang KY, Sistermans E, Rauch A, Niemeyer CM, Shannon K, Kratz CP: Germline KRAS mutations cause Noonan syndrome. Nat Genet 2006;38:331-336.
-
(2006)
Nat Genet
, vol.38
, pp. 331-336
-
-
Schubbert, S.1
Zenker, M.2
Rowe, S.L.3
Boll, S.4
Klein, C.5
Bollag, G.6
van der Burgt, I.7
Musante, L.8
Kalscheuer, V.9
Wehner, L.E.10
Nguyen, H.11
West, B.12
Zhang, K.Y.13
Sistermans, E.14
Rauch, A.15
Niemeyer, C.M.16
Shannon, K.17
Kratz, C.P.18
-
9
-
-
33845884026
-
Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome
-
Tartaglia M, Pennacchio LA, Zhao C, Yadav KK, Fodale V, Sarkozy A, Pandit B, Oishi K, Martinelli S, Schackwitz W, Ustaszewska A, Martin J, Bristow J, Carta C, Lepri F, Neri C, Vasta I, Gibson K, Curry CJ, Siguero JP, Digilio MC, Zampino G, Dallapiccola B, Bar-Sagi D, Gelb BD: Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome. Nat Genet 2007;39:75-79.
-
(2007)
Nat Genet
, vol.39
, pp. 75-79
-
-
Tartaglia, M.1
Pennacchio, L.A.2
Zhao, C.3
Yadav, K.K.4
Fodale, V.5
Sarkozy, A.6
Pandit, B.7
Oishi, K.8
Martinelli, S.9
Schackwitz, W.10
Ustaszewska, A.11
Martin, J.12
Bristow, J.13
Carta, C.14
Lepri, F.15
Neri, C.16
Vasta, I.17
Gibson, K.18
Curry, C.J.19
Siguero, J.P.20
Digilio, M.C.21
Zampino, G.22
Dallapiccola, B.23
Bar-Sagi, D.24
Gelb, B.D.25
more..
-
10
-
-
33845900943
-
Germline gain-of-function mutations in SOS1 cause Noonan syndrome
-
Roberts AE, Araki T, Swanson KD, Montgomery KT, Schiripo TA, Joshi VA, Li L, Yassin Y, Tamburino AM, Neel BG, Kucherlapati RS: Germline gain-of-function mutations in SOS1 cause Noonan syndrome. Nat Genet 2007;39:70-74.
-
(2007)
Nat Genet
, vol.39
, pp. 70-74
-
-
Roberts, A.E.1
Araki, T.2
Swanson, K.D.3
Montgomery, K.T.4
Schiripo, T.A.5
Joshi, V.A.6
Li, L.7
Yassin, Y.8
Tamburino, A.M.9
Neel, B.G.10
Kucherlapati, R.S.11
-
11
-
-
34547539552
-
Germline gain-of-function mutations in RAF1 cause Noonan syndrome
-
Razzaque MA, Nishizawa T, Komoike Y, Yagi H, Furutani M, Amo R, Kamisago M, Momma K, Katayama H, Nakagawa M, Fujiwara Y, Matsushima M, Mizuno K, Tokuyama M, Hirota H, Muneuchi J, Higashinakagawa T, Matsuoka R: Germline gain-of-function mutations in RAF1 cause Noonan syndrome. Nat Genet 2007;39:1013-1017.
-
(2007)
Nat Genet
, vol.39
, pp. 1013-1017
-
-
Razzaque, M.A.1
Nishizawa, T.2
Komoike, Y.3
Yagi, H.4
Furutani, M.5
Amo, R.6
Kamisago, M.7
Momma, K.8
Katayama, H.9
Nakagawa, M.10
Fujiwara, Y.11
Matsushima, M.12
Mizuno, K.13
Tokuyama, M.14
Hirota, H.15
Muneuchi, J.16
Higashinakagawa, T.17
Matsuoka, R.18
-
12
-
-
34547530823
-
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy
-
Pandit B, Sarkozy A, Pennacchio LA, Carta C, Oishi K, Martinelli S, Pogna EA, Schackwitz W, Ustaszewska A, Landstrom A, Bos JM, Ommen SR, Esposito G, Lepri F, Faul C, Mundel P, López Siguero JP, Tenconi R, Selicorni A, Rossi C, Mazzanti L, Torrente I, Marino B, Digilio MC, Zampino G, Ackerman MJ, Dallapiccola B, Tartaglia M, Gelb BD: Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy. Nat Genet 2007; 39:1007-1012.
-
(2007)
Nat Genet
, vol.39
, pp. 1007-1012
-
-
Pandit, B.1
Sarkozy, A.2
Pennacchio, L.A.3
Carta, C.4
Oishi, K.5
Martinelli, S.6
Pogna, E.A.7
Schackwitz, W.8
Ustaszewska, A.9
Landstrom, A.10
Bos, J.M.11
Ommen, S.R.12
Esposito, G.13
Lepri, F.14
Faul, C.15
Mundel, P.16
López Siguero, J.P.17
Tenconi, R.18
Selicorni, A.19
Rossi, C.20
Mazzanti, L.21
Torrente, I.22
Marino, B.23
Digilio, M.C.24
Zampino, G.25
Ackerman, M.J.26
Dallapiccola, B.27
Tartaglia, M.28
Gelb, B.D.29
more..
-
13
-
-
4043056497
-
Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpnll mutation
-
Araki T, Mohi MG, Ismat FA, Bronson RT, Williams IR, Kutok JL, Yang W, Pao LI, Gilliland DG, Epstein JA, Neel BG: Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpnll mutation. Nat Med 2004;10:849-857.
-
(2004)
Nat Med
, vol.10
, pp. 849-857
-
-
Araki, T.1
Mohi, M.G.2
Ismat, F.A.3
Bronson, R.T.4
Williams, I.R.5
Kutok, J.L.6
Yang, W.7
Pao, L.I.8
Gilliland, D.G.9
Epstein, J.A.10
Neel, B.G.11
-
14
-
-
33644696097
-
Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome
-
Rodriguez-Viciana P, Tetsu O, Tidyman WE, Estep AL, Conger BA, Cruz MS, McCormick F, Rauen KA: Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome. Science 2006; 311:1287-1290.
-
(2006)
Science
, vol.311
, pp. 1287-1290
-
-
Rodriguez-Viciana, P.1
Tetsu, O.2
Tidyman, W.E.3
Estep, A.L.4
Conger, B.A.5
Cruz, M.S.6
McCormick, F.7
Rauen, K.A.8
-
15
-
-
35348871857
-
SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome
-
Zenker M, Horn D, Wieczorek D, Allanson J, Pauli S, van der Burgt I, Doerr HG, Caspar H, Hofbeck M, Gillessen-Kaesbach G, Koch A, Meinecke P, Mundlos S, Nowka A, Rauch A, Reif S, von Schnakenburg C, Seidel H, Wehner LE, Zweier C, Bauhuber S, Matejas V, Kratz CP, Thomas C, Kutsche K: SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome. J Med Genet 2007;44:651-656.
-
(2007)
J Med Genet
, vol.44
, pp. 651-656
-
-
Zenker, M.1
Horn, D.2
Wieczorek, D.3
Allanson, J.4
Pauli, S.5
van der Burgt, I.6
Doerr, H.G.7
Caspar, H.8
Hofbeck, M.9
Gillessen-Kaesbach, G.10
Koch, A.11
Meinecke, P.12
Mundlos, S.13
Nowka, A.14
Rauch, A.15
Reif, S.16
von Schnakenburg, C.17
Seidel, H.18
Wehner, L.E.19
Zweier, C.20
Bauhuber, S.21
Matejas, V.22
Kratz, C.P.23
Thomas, C.24
Kutsche, K.25
more..
-
16
-
-
20144389353
-
Genotypic and phenotypic characterization of Noonan syndrome: New data and review of the literature
-
Jongmans M, Sistermans EA, Rikken A, Nillesen WM, Tamminga R, Patton M, Maier EM, Tartaglia M, Noordam K, van der Burgt I: Genotypic and phenotypic characterization of Noonan syndrome: new data and review of the literature. Am J Med Genet 2005;134:165-170.
-
(2005)
Am J Med Genet
, vol.134
, pp. 165-170
-
-
Jongmans, M.1
Sistermans, E.A.2
Rikken, A.3
Nillesen, W.M.4
Tamminga, R.5
Patton, M.6
Maier, E.M.7
Tartaglia, M.8
Noordam, K.9
van der Burgt, I.10
-
17
-
-
0024238928
-
Noonan syndrome: Growth and clinical manifestations in 144 cases
-
Ranke MB, Heidemann P, Knupfer C, Enders H, Schmaltz AA, Bierich JR: Noonan syndrome: growth and clinical manifestations in 144 cases. Eur J Pediatr 1988; 148:220-227.
-
(1988)
Eur J Pediatr
, vol.148
, pp. 220-227
-
-
Ranke, M.B.1
Heidemann, P.2
Knupfer, C.3
Enders, H.4
Schmaltz, A.A.5
Bierich, J.R.6
-
18
-
-
33847075012
-
The natural history of Noonan syndrome: A long-term follow-up study
-
Shaw AC, Kalidas K, Crosby AH, Jeffery S, Patton MA: The natural history of Noonan syndrome: a long-term follow-up study. Arch Dis Child 2007;92:128-132.
-
(2007)
Arch Dis Child
, vol.92
, pp. 128-132
-
-
Shaw, A.C.1
Kalidas, K.2
Crosby, A.H.3
Jeffery, S.4
Patton, M.A.5
-
20
-
-
0026073598
-
Noonan's syndrome: Abnormalities of the growth hor-mone/IGF-I axis and the response to treatment with human biosynthetic growth hormone
-
Ahmed ML, Foot AB, Edge JA, Lamkin VA, Savage MO, Dunger DB: Noonan's syndrome: abnormalities of the growth hor-mone/IGF-I axis and the response to treatment with human biosynthetic growth hormone. Acta Paediatr Scand 1991;80:446-450.
-
(1991)
Acta Paediatr Scand
, vol.80
, pp. 446-450
-
-
Ahmed, M.L.1
Foot, A.B.2
Edge, J.A.3
Lamkin, V.A.4
Savage, M.O.5
Dunger, D.B.6
-
21
-
-
0035131555
-
Growth hormone (GH) secretion in children with Noonan syndrome: Frequently abnormal without consequences for growth or response to GH treatment
-
Noordam C, van der Burgt I, Sweep CG, Delemarrevan de Waal HA, Sengers RC, Otten BJ: Growth hormone (GH) secretion in children with Noonan syndrome: frequently abnormal without consequences for growth or response to GH treatment. Clin Endocrinol 2001;54:53-59.
-
(2001)
Clin Endocrinol
, vol.54
, pp. 53-59
-
-
Noordam, C.1
van der Burgt, I.2
Sweep, C.G.3
Delemarrevan de Waal, H.A.4
Sengers, R.C.5
Otten, B.J.6
-
22
-
-
0031890381
-
Involvement of the Src homology 2-containing tyrosine phosphatase SHP2 in growth hormone signalling
-
Kim SO, Jiang J, Yi W, Feng GS, Frank SJ: Involvement of the Src homology 2-containing tyrosine phosphatase SHP2 in growth hormone signalling. J Biol Chem 1998;273: 2344-2354.
-
(1998)
J Biol Chem
, vol.273
, pp. 2344-2354
-
-
Kim, S.O.1
Jiang, J.2
Yi, W.3
Feng, G.S.4
Frank, S.J.5
-
23
-
-
0034614626
-
Cytosolic tyrosine dephosphorylation of STAT5
-
Yu C-L, Yong-Jiu J, Burakoff SJ: Cytosolic tyrosine dephosphorylation of STAT5. J Biol Chem 2000;275:599-604.
-
(2000)
J Biol Chem
, vol.275
, pp. 599-604
-
-
Yu, C.-L.1
Yong-Jiu, J.2
Burakoff, S.J.3
-
24
-
-
0037593839
-
Identification of SHP2 as a Stat5a phosphatase
-
Chen Y, Wen R, Yang S, Schuman J, Zhang EE, Yi T, Feng G-S, Wang D: Identification of SHP2 as a Stat5a phosphatase. J Biol Chem 2003;278:16520- 16527.
-
(2003)
J Biol Chem
, vol.278
, pp. 16520-16527
-
-
Chen, Y.1
Wen, R.2
Yang, S.3
Schuman, J.4
Zhang, E.E.5
Yi, T.6
Feng, G.-S.7
Wang, D.8
-
25
-
-
0033755417
-
Mutation of the SHP2 binding site in growth hormone (GH) receptor prolongs GH-promoted tyrosyl phosphorylation of GH receptor, JAK2, and STAT5B
-
Stofega MR, Herrington J, Billestrup N, Carter-Su C: Mutation of the SHP2 binding site in growth hormone (GH) receptor prolongs GH-promoted tyrosyl phosphorylation of GH receptor, JAK2, and STAT5B. Mol Endocrinol 2000;14:1338-1350.
-
(2000)
Mol Endocrinol
, vol.14
, pp. 1338-1350
-
-
Stofega, M.R.1
Herrington, J.2
Billestrup, N.3
Carter-Su, C.4
-
26
-
-
24344436765
-
PTPN11 mutations are associated with mild growth hormone resistance in individuals with Noonan syndrome
-
Binder G, Neuer K, Ranke MB, Wittekindt NE: PTPN11 mutations are associated with mild growth hormone resistance in individuals with Noonan syndrome. J Clin Endocrinol Metab 2005;90:5377-5381.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 5377-5381
-
-
Binder, G.1
Neuer, K.2
Ranke, M.B.3
Wittekindt, N.E.4
-
27
-
-
24344470070
-
PTPN11 mutations and response to growth hormone therapy in children with Noonan syndrome
-
Ferreira LV, Souza SAL, Arnhold IJP, Mendonca BB, Jorge AAL: PTPN11 mutations and response to growth hormone therapy in children with Noonan syndrome. J Clin Endocrinol Metab 2005;90:5156-5160.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 5156-5160
-
-
Ferreira, L.V.1
Souza, S.A.L.2
Arnhold, I.J.P.3
Mendonca, B.B.4
Jorge, A.A.L.5
-
28
-
-
30344444283
-
Noonan syndrome: Relationships between genotype, growth, and growth factors
-
Limal J-M, Parfait B, Cabrol S, Bonnet D, Leheup B, Lyonnet S, Vidaud M, Le Bouc Y: Noonan syndrome: relationships between genotype, growth, and growth factors. J Clin Endocrinol Metab 2006;91:300-306.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 300-306
-
-
Limal, J.-M.1
Parfait, B.2
Cabrol, S.3
Bonnet, D.4
Leheup, B.5
Lyonnet, S.6
Vidaud, M.7
Le Bouc, Y.8
-
29
-
-
0035008529
-
Growth hormone therapy and growth in children with Noonan's syndrome: Results of 3 years' follow-up
-
MacFarlane CE, Brown DC, Johnston LB, Patton MA, Dunger DB, Savage MO, Mc-Kenna WJ, Kelnar CJ: Growth hormone therapy and growth in children with Noonan's syndrome: results of 3 years' follow-up. J Clin Endocrinol Metab 2001;86:1953-1956.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 1953-1956
-
-
MacFarlane, C.E.1
Brown, D.C.2
Johnston, L.B.3
Patton, M.A.4
Dunger, D.B.5
Savage, M.O.6
Mc-Kenna, W.J.7
Kelnar, C.J.8
-
30
-
-
0034881311
-
Growth hormone treatment in children with Noonan's syndrome: Four year results of a partly controlled trial
-
Noordam C, van der Burgt I, Sengers RCA, Delemarrevan de Waal HA, Otten BJ: Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trial. Acta Paediatr 2001; 90:889-894.
-
(2001)
Acta Paediatr
, vol.90
, pp. 889-894
-
-
Noordam, C.1
van der Burgt, I.2
Sengers, R.C.A.3
Delemarrevan de Waal, H.A.4
Otten, B.J.5
-
31
-
-
27144487822
-
Improved final height with long-term growth hormone treatment in Noonan syndrome
-
Osio D, Dahlgren J, Albertsson Wikland K, Westphal O: Improved final height with long-term growth hormone treatment in Noonan syndrome. Acta Paediatr 2005;94: 1232-1237.
-
(2005)
Acta Paediatr
, vol.94
, pp. 1232-1237
-
-
Osio, D.1
Dahlgren, J.2
Albertsson Wikland, K.3
Westphal, O.4
-
32
-
-
24744455046
-
The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease
-
Kratz CP, Niemeyer CM, Castleberry RP, Cetin M, Bergsträsser E, Emanuel PD, Hasle H, Kardos G, Klein C, Kojima S, Stary J, Trebo M, Zecca M, Gelb BD, Tartaglia M, Loh ML: The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease. Blood 2005;106:2183-2185.
-
(2005)
Blood
, vol.106
, pp. 2183-2185
-
-
Kratz, C.P.1
Niemeyer, C.M.2
Castleberry, R.P.3
Cetin, M.4
Bergsträsser, E.5
Emanuel, P.D.6
Hasle, H.7
Kardos, G.8
Klein, C.9
Kojima, S.10
Stary, J.11
Trebo, M.12
Zecca, M.13
Gelb, B.D.14
Tartaglia, M.15
Loh, M.L.16
-
33
-
-
18444394019
-
A new PTPN11 mutation in juvenile myelomonocytic leukaemia associated with Noonan syndrome
-
Giovannini L, Cavé H, Ferrero-Vacher C, Boutte P, Sirvent N: A new PTPN11 mutation in juvenile myelomonocytic leukaemia associated with Noonan syndrome. Acta Paediatr 2005;94:636-637.
-
(2005)
Acta Paediatr
, vol.94
, pp. 636-637
-
-
Giovannini, L.1
Cavé, H.2
Ferrero-Vacher, C.3
Boutte, P.4
Sirvent, N.5
-
34
-
-
34247137902
-
Respiratory failure, juvenile myelomonocytic leukemia, and neonatal Noonan syndrome
-
Cheong JL, Moorkamp MH: Respiratory failure, juvenile myelomonocytic leukemia, and neonatal Noonan syndrome. J Pediatr Hematol Oncol 2007;29:262-264.
-
(2007)
J Pediatr Hematol Oncol
, vol.29
, pp. 262-264
-
-
Cheong, J.L.1
Moorkamp, M.H.2
-
35
-
-
18244395853
-
Human somatic PTPN11 mutations induce hemato-poietic-cell hypersensitivity to granulocyte-macrophage colony-stimulating factor
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Chan RJ, Leedy MB, Munugalavadla V, Voorhorst CS, Li Y, Yu M, Kapur R: Human somatic PTPN11 mutations induce hemato-poietic-cell hypersensitivity to granulocyte-macrophage colony-stimulating factor. Blood 2005;105:3737-3742.
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(2005)
Blood
, vol.105
, pp. 3737-3742
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Chan, R.J.1
Leedy, M.B.2
Munugalavadla, V.3
Voorhorst, C.S.4
Li, Y.5
Yu, M.6
Kapur, R.7
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